ResearcherUniversity of CologneActive in the last 2 years
Thomas Schmidt
Matched on ORCID iD 0000-0002-0045-1851; OpenAlex author ID A5100698425. Sources: OpenAlex.
Their work
- Papers
- 9 (first author 0, last author 1)
- Trials
- 0
- Grants
- 0
- Labs led
- 0
- Collaborators
- 35
2017: 1 paper · 2018: none · 2019: 3 papers · 2020: none · 2021: none · 2022: none · 2023: 1 paper · 2024: 4 papers
Papers 9
- Differential Sensitivity to Ionizing Radiation in Gemcitabine-Resistant and Paclitaxel-Resistant Pancreatic Cancer Cells. Co-author DOI 10.1016/j.ijrobp.2023.10.035↗
- Extent and clinical significance of the therapy-relevant tight junction protein Claudin 18.2 in pancreatic ductal adenocarcinoma - real-world evidence. Co-author DOI 10.1016/j.tranon.2024.102044↗
- ABCB1 overexpression through locus amplification represents an actionable target to combat paclitaxel resistance in pancreatic cancer cells. Co-author DOI 10.1186/s13046-023-02879-8↗
- Altered Mechanobiology of PDAC Cells with Acquired Chemoresistance to Gemcitabine and Paclitaxel. Last author DOI 10.3390/cancers16223863↗
- Prognostic Significance of Integrin Subunit Alpha 2 (ITGA2) and Role of Mechanical Cues in Resistance to Gemcitabine in Pancreatic Ductal Adenocarcinoma (PDAC). Co-author DOI 10.3390/cancers15030628↗
- A mechanical memory of pancreatic cancer cells Co-author DOI 10.1101/730960↗
- The Activity of Kv 11.1 Potassium Channel Modulates F-Actin Organization During Cell Migration of Pancreatic Ductal Adenocarcinoma Cells. Co-author DOI 10.3390/cancers11020135↗
- Role of c-MET Inhibitors in Overcoming Drug Resistance in Spheroid Models of Primary Human Pancreatic Cancer and Stellate Cells. Co-author DOI 10.3390/cancers11050638↗
- A mechanopharmacology approach to overcome chemoresistance in pancreatic cancer. Co-author DOI 10.1016/j.drup.2017.07.001↗
Closest collaborators
The 25 strongest of 35 by collab_strength@1: shared papers, trials and grants, recent and small-team work weighing most.
- Elisa Giovannetti · 7 shared papers, 2017–2024 · strength 1.05
- Paper Altered Mechanobiology of PDAC Cells with Acquired Chemoresistance to Gemcitabine and Paclitaxel. DOI 10.3390/cancers16223863↗
- Paper Differential Sensitivity to Ionizing Radiation in Gemcitabine-Resistant and Paclitaxel-Resistant Pancreatic Cancer Cell… DOI 10.1016/j.ijrobp.2023.10.035↗
- Paper ABCB1 overexpression through locus amplification represents an actionable target to combat paclitaxel resistance in pan… DOI 10.1186/s13046-023-02879-8↗
- Erik H.J. Danen · 5 shared papers, 2017–2024 · strength 0.84
- Paper Altered Mechanobiology of PDAC Cells with Acquired Chemoresistance to Gemcitabine and Paclitaxel. DOI 10.3390/cancers16223863↗
- Paper Differential Sensitivity to Ionizing Radiation in Gemcitabine-Resistant and Paclitaxel-Resistant Pancreatic Cancer Cell… DOI 10.1016/j.ijrobp.2023.10.035↗
- Paper ABCB1 overexpression through locus amplification represents an actionable target to combat paclitaxel resistance in pan… DOI 10.1186/s13046-023-02879-8↗
- Cecilia Bergonzini · 4 shared papers, 2023–2024 · strength 0.76
- Paper Altered Mechanobiology of PDAC Cells with Acquired Chemoresistance to Gemcitabine and Paclitaxel. DOI 10.3390/cancers16223863↗
- Paper Differential Sensitivity to Ionizing Radiation in Gemcitabine-Resistant and Paclitaxel-Resistant Pancreatic Cancer Cell… DOI 10.1016/j.ijrobp.2023.10.035↗
- Paper ABCB1 overexpression through locus amplification represents an actionable target to combat paclitaxel resistance in pan… DOI 10.1186/s13046-023-02879-8↗
- Alessandro Gregori · 4 shared papers, 2023–2024 · strength 0.76
- Paper Altered Mechanobiology of PDAC Cells with Acquired Chemoresistance to Gemcitabine and Paclitaxel. DOI 10.3390/cancers16223863↗
- Paper Differential Sensitivity to Ionizing Radiation in Gemcitabine-Resistant and Paclitaxel-Resistant Pancreatic Cancer Cell… DOI 10.1016/j.ijrobp.2023.10.035↗
- Paper ABCB1 overexpression through locus amplification represents an actionable target to combat paclitaxel resistance in pan… DOI 10.1186/s13046-023-02879-8↗
- Mjriam Capula · 4 shared papers, 2019–2024 · strength 0.70
- Paper Altered Mechanobiology of PDAC Cells with Acquired Chemoresistance to Gemcitabine and Paclitaxel. DOI 10.3390/cancers16223863↗
- Paper ABCB1 overexpression through locus amplification represents an actionable target to combat paclitaxel resistance in pan… DOI 10.1186/s13046-023-02879-8↗
- Paper Prognostic Significance of Integrin Subunit Alpha 2 (ITGA2) and Role of Mechanical Cues in Resistance to Gemcitabine in… DOI 10.3390/cancers15030628↗
- Stefano Coppola · 4 shared papers, 2017–2019 · strength 0.37
- Paper A mechanical memory of pancreatic cancer cells DOI 10.1101/730960↗
- Paper The Activity of Kv 11.1 Potassium Channel Modulates F-Actin Organization During Cell Migration of Pancreatic Ductal Ade… DOI 10.3390/cancers11020135↗
- Paper Role of c-MET Inhibitors in Overcoming Drug Resistance in Spheroid Models of Primary Human Pancreatic Cancer and Stella… DOI 10.3390/cancers11050638↗
- Liam Andrew McDonnell · 2 shared papers, 2024 · strength 0.36
- Paper Differential Sensitivity to Ionizing Radiation in Gemcitabine-Resistant and Paclitaxel-Resistant Pancreatic Cancer Cell… DOI 10.1016/j.ijrobp.2023.10.035↗
- Paper ABCB1 overexpression through locus amplification represents an actionable target to combat paclitaxel resistance in pan… DOI 10.1186/s13046-023-02879-8↗
- Ilaria Carnevale · 3 shared papers, 2017–2019 · strength 0.28
- Paper A mechanical memory of pancreatic cancer cells DOI 10.1101/730960↗
- Paper Role of c-MET Inhibitors in Overcoming Drug Resistance in Spheroid Models of Primary Human Pancreatic Cancer and Stella… DOI 10.3390/cancers11050638↗
- Paper A mechanopharmacology approach to overcome chemoresistance in pancreatic cancer. DOI 10.1016/j.drup.2017.07.001↗
- Pei Pei · 2 shared papers, 2019–2024 · strength 0.27
- Paper Differential Sensitivity to Ionizing Radiation in Gemcitabine-Resistant and Paclitaxel-Resistant Pancreatic Cancer Cell… DOI 10.1016/j.ijrobp.2023.10.035↗
- Paper Role of c-MET Inhibitors in Overcoming Drug Resistance in Spheroid Models of Primary Human Pancreatic Cancer and Stella… DOI 10.3390/cancers11050638↗
- Alexander Ioannis Damanakis · 1 shared paper, 2024 · strength 0.20
- Felix Popp · 1 shared paper, 2024 · strength 0.20
- Alexander Quaas · 1 shared paper, 2024 · strength 0.20
- Su Ir Lyu · 1 shared paper, 2024 · strength 0.20
- Karl Knipper · 1 shared paper, 2024 · strength 0.20
- Dirk Waldschmidt · 1 shared paper, 2024 · strength 0.20
- Christiane J. Bruns · 1 shared paper, 2024 · strength 0.20
- Adam Enver Frampton · 1 shared paper, 2024 · strength 0.18
- Asia Botto · 1 shared paper, 2024 · strength 0.18
- Ingrid Garajová · 1 shared paper, 2024 · strength 0.18
- Annalisa Comandatore · 1 shared paper, 2023 · strength 0.16
- Fatemeh Khojasteh‐Leylakoohi · 1 shared paper, 2023 · strength 0.16
- Luca Morelli · 1 shared paper, 2023 · strength 0.16
- Amir Avan · 1 shared paper, 2023 · strength 0.16
- Godefridus J. Peters · 2 shared papers, 2017–2019 · strength 0.16
- Sagar S. Manoli · 1 shared paper, 2019 · strength 0.09
How to reach this person
A chain of introductions through people who have published, run trials or held grants together (warm_path@1: fewest links first, then the strongest). Built from public records only; no contact details are kept.